Функциональные ответы альвеолярных макрофагов, сурфактантный белок D и заболевания легких
https://doi.org/10.18093/0869-0189-2011-0-3-101-107
Аннотация
Функциональные ответы альвеолярных макрофагов, сурфактантный белок D и заболевания легких.
Ключевые слова
Об авторах
И. Ю. МалышевРоссия
д. м. н., проф., зав. лабораторией клеточных биотехнологий, зав. лабораторией стресса и адаптацией
127473, Москва, ул. Делегатская, 20 / 1
25315, Москва, ул. Балтийская, 8. Тел.: +7-985-766-24-40.
С. В. Лямина
Россия
к. м. н., старший научный сотрудник лаборатории клеточных биотехнологий
127473, Москва, ул. Делегатская, 20 / 1. Тел.: +7-915-018-50-06.
Ш. Л. Шимшелашвили
Россия
к. м. н., ассистент кафедры госпитальной терапевтической стоматологии, пародонтологии и гериатрической стоматологии
127473, Москва, ул. Делегатская, 20 / 1. Тел.: +7-985-766-24-40.
Е. Н. Вассерман
Соединённые Штаты Америки
к. м. н., старший научный сотрудник Школы медицины, отделения легочной и интенсивной терапии
Vernon and Shirley Hill Pavilion, # H410C 380 S. University Ave. Philadelphia, PA 19104-4539. Тел.: +7-985-766-24-40.
Список литературы
1. Чучалин А.Г. (ред.). Стандарты по диагностике и лечению больных хронической обструктивной болезнью легких (ATS / ERS, пересмотр 2004 г.). Пер. с англ. М.: Атмосфера; 2005.
2. Хаитов Р.М. Иммунология: Учебник. М.: ГЭОТАР-Медиа; 2006.
3. Janeway C.A., Travers P., Walport M., Shlomchik M. Immunobiology. The immune system in health and disease: New York: Garland Science Publishing, 2005.
4. Mantovani A., Sica A., Sozzani S. et al. The chemokine system in diverse forms of macrophage activation and polarization. Trends Immunol. 2004; 25: 677–686.
5. Mantovani A. Macrophage diversity and polarization: in vivo veritas. Blood 2006; 108 (2): 408–409.
6. Mantovani A., Sica A., Locatti A. New vistas on macrophage differentiation and activation. Eur. J. Immunol. 2006; 37 (1): 14–16.
7. Boehm U., Klamp T., Groot M., Howard J.C. Cellular responses to interferon-gamma. Ann. Rev. Immunol. 1997; 15: 749–795.
8. Sharma M. Chemokines and their receptors: orchestrating a fine balance between health and disease. Crit. Rev. Biotechnol. 2010; 30: 1–22.
9. Trost M., English L., Limieux S. et al. The phagosomal proteome in interferon-?-activated macrophages. Immunity 2009; 30 (1): 143–154.
10. Nelson S. Novel nonantibiotic therapies for pneumonia. Cytokines and host defence. Chest 2001; 119 (2): 419S–425S.
11. Martinez F.O., Gordon S., Locati A., Mantovani A. Transcriptional profiling of the human monocyte-to-macrophage differentiation and polarization: New molecules and patterns of gene expression. J. Immunol. 2006; 177: 7303–7311.
12. Kaplan A.P. Chemokines, chemokine receptors and allergy. Int. Arch. Allergy Immunol. 2001; 124 (4): 423–431.
13. Falcone F.H., Haas H., Gibbs B.F. The human basophil: a new appreciation of its role in immune responses. Blood 2000; 96 (13): 4028–4038.
14. D'Andrea A., Aste5Amezaga M., Valiante N.M. et al. Interleukin 10 (IL-10) inhibits human lymphocyte interferon gamma-production by suppressing natural killer cell stimulatory factor / IL-12 synthesis in accessory cells. J. Exp. Med. 1993; 178 (3): 1041–1048.
15. Hu S., Sheng W.S., Peterson P.K., Chao C.C. Differential regulation by cytokines of production of nitric oxide by human astrocytes. Glia 1995; 15: 491–494.
16. Gordon S. The macrophage: Past, present and future. Eur. J. Immunol. 2007; 37: S9.
17. Martinez F.O., Sica A., Mantovani A., Locati M. Macrophage activation and polarization. Front. Biosci. 2008; 1 (13): 453–461.
18. Sieling P.A., Abrams J.S., Yamamura M. et al. Immunosuppressive roles for IL-10 and IL-4 in human infection. In vitro modulation of T cell responses in leprosy. J. Immunol. 1993; 150 (12): 5501–5510.
19. Oosterhout A.J.M., Motta A.C. Th1 / Th2 paradigm: not seeing the forest for the trees? Eur. Respir. J. 2005; 25: 591–593.
20. Mantovani A., Sozzani S., Locati M. et al. Macrophage polarization: tumor-associated macrophages as a paradigm for polarized M2 mononuclear phagocytes. Trends Immunol. 2002; 23 (11): 549–555.
21. Fritz J., Murphy B.S., Sundareshan V. et al. M1 and M2 Macrophage activation. Azithromycin alters macrophage phenotype. J. Antimicrob. Chemother. 2008; 61 (3): 554–560.
22. Atochina E.N., Beck J.M., Scanlon S.T. et al. Pneumocystis carinii pneumonia alters expression and distribution of lung collectins SP-A and SP-D. J. Lab. Clin. Med. 2001; 137: 429–39.
23. Atochina E.N., Beers M.F., Hawgood S. et al. Surfactant protein-D, a mediator of innate lung immunity, alters the products of nitric oxide metabolism. Am. J. Respir. Cell Mol. Biol. 2004; 30: 271–279.
24. Cheng G., Ueda T., Numao T. et al. Increased levels of surfactant protein A and D in bronchoalveolar lavage fluids in patients with bronchial asthma. Eur. Respir. J. 2000; 16: 831–835.
25. Cheng I.W., Ware L.B., Greene K.E. et al. Prognostic value of surfactant proteins A and D in patients with acute lung injury. Crit. Care Med. 2003; 31: 20–27.
26. Eisner M.D., Parsons P., Matthay M.A. et al. Plasma surfactant protein levels and clinical outcomes in patients with acute lung injury. Thorax 2003; 58: 983–988.
27. Fujita M., Shannon J.M., Ouchi H. et al. Serum surfactant protein D is increased in acute and chronic inflammation in mice. Cytokine 2005; 31: 25–33.
28. Kuan S., Rust K., Crouch E. Interactions of surfactant protein D with bacterial lipopolysaccharides. J. Clin. Invest. 1992; 90: 97–106.
29. Wright J.R. Immunomodulatory functions of surfactant. Physiol. Rev. 1997; 77: 931–962.
30. Crouch E.C. Structure, biologic properties and expression of surfactant protein D. Biochim. Biophys. Acta 1998; 1408: 278–289.
31. Sorensen G.L., Husby S., Holmskov U. Surfactant protein A and surfactant protein D variation in pulmonary disease. Immunobiology 2007; 212 (4–5): 381–416.
32. Sin D.D., Pahlavan P.S., Man P.S.P. Surfactant protein D: A lung specific biomarker in COPD?: Potential biological roles of SP-D in COPD. Ther. Adv. Respir Dis. 2008; 2 (2): 65–74.
33. Fisher J.H., Larson J., Cool C., Dow S.W. Lymphocyte activation in the lungs of SP-D null mice. Am. J. Respir. Cell. Mol. Biol. 2002; 27: 24–33.
34. Botas C.F., Poulain J., Akiyama J. et al. Altered surfactant homeostasis and alveolar type II cell morphology in mice lacking surfactant protein D. Proc. Natl. Acad. Sci. USA 1998; 95:11869–11874.
35. Wert S.E., Yoshida M., LeVine A.M. et al. Increased metalloproteinase activity, oxidant production, and emphysema in surfactant protein D gene-inactivated mice. Proc. Natl. Acad. Sci. USA 1997; 97: 5972–5977.
36. Korfhagen T.R., Sheftelyevich V., Burhans M.S. et al. Surfactant protein-D regulates surfactant phospholipid homeostasis in vivo. J. Biol. Chem. 1998; 273: 28438–28443.
37. Yoshida M., Korfhagen Th.R., Whitsett J.A. Surfactant protein D regulates NF-κB and matrix metalloproteinase production in alveolar macrophages via oxidant-sensitive pathways. J. Immunol. 2001; 166: 7514–7519.
38. LeVine A.M., Whitsett J.A., Gwozdz J.A. et al. Distinct effects of surfactant protein A or D deficiency during bacterial infection on the lung. J. Immunol. 2000; 165: 3934–3940.
39. Gardai S.J., Xiao Y.5Q., Dickinson M. et al. By binding SIRP-alpha or calreticulin / CD91, lung collectins act as dual function surveillance molecules to suppress or enhance inflammation. Cell 2003; 115: 13–23.
40. Atochina5Vasserman E.N., Kadire H., Tomer Y. et al. Selective inhibition of iNOS activity in vivo reverses inflammatory abnormalities in SP-D deficient mice. J. Immunol. 2007; 179 (12): 8090–8097.
41. Atochina5Vasserman E.N., Abramova E.V., Tomer Y. et al. SP-D-Dependent regulation of NO metabolism in lipopolysaccharide-stimulated peritoneal macrophages. Bull. Exp. Biol. Med. 2009; 147 (4): 415–420.
42. Sano H., Kuroki Y. The lung collectins, SP-A and SP-D, modulate pulmonary innate immunity. Mol. Immunol. 2005; 42 (3): 279–287.
43. Guo C.J., Atochina5Vasserman E.N., Abramova H. et al. S-Nitrosylation of surfactant protein-D controls inflammatory function. PLoS Biol. 2008; 6 (11): e266.
44. Zhang L., Ikegami M., Crouch E.C. et al. Activity of pulmonary surfactant protein-D (SP-D) in vivo is dependent on oligomeric structure. J. Biol. Chem. 2001; 276 (22): 19214–19219.
45. Guo C.J., Rashman C.S., Wolf B.A., Gow A.J. S-Nitrosylation of surfactant protein-D provides a molecular switch from anti- to pro-inflammatory function. Nitric Oxide 2006; 14 (4): 6.
46. McCormack F.X., Whitsett J.A. The pulmonary collectins, SP-A and SP-D, orchestrate innate immunity in the lung. J. Clin. Invest 2002; 109 (6): 707–712.
47. Bartlett J.G., Breiman R.F., Mandell L.A. et al. Communityacquired pneumonia in adults-guidelines for management. Clin. Infect. Dis. 1998; 26: 811–838.
48. Bufler P., Schikor D., Schmidt B., Griese M. Cytokine stimulation by Pseudomonas aeruginosa strain variation and modulation by pulmonary surfactant. Exp. Lung Res. 2004; 30 (3): 163–179.
49. Lofdahl M., Wahlstorm J., Skold C.M. Different inflammatory cell pattern and macrophage phenotype in chronic obstructive pulmonary disease patients, smokers and non-smokers. Clin. Exp. Immunol. 2006; 145 (3): 428–437.
50. Pons A.R., Noguera A., Blanquer D. et al. Phenotypic characterization of alveolar macrophages and peripheral blood monocytes in COPD. Eur. Respir. J. 2005; 25 (4): 647–652.
51. Shaykhiev R., Krause A., Salit J. et al. Smoking-dependent reprogramming of alveolar macrophage polarization: implication for pathogenesis of chronic obstructive pulmonary disease. J. Immunol. 2009; 183: 2867–2883.
52. Лещенко И.В. Глобальная инициатива по хронической обструктивной болезни легких: новые направления в лечении. Урал. мед. Журн. 2006; 8 (36).
53. Sethi S., Maloney J., Grove L. et al. Airway inflammation and bronchial bacterial colonization in chronic obstructive pulmonary disease. Res. Med. COPD Update 2006; 1 (4): 144–145.
54. Доклад экспертов ВОЗ; 2005.
55. Woodruff P.G., Modrek B., Choy D.F. et al. T-helper type 2-driven inflammation defines major subphenotypes of asthma. Am. J. Respir. Crit. Care Med. 2009; 180 (5): 388–395.
56. Шмелев Е.И. Дифференциальная диагностика интерстициальных заболеваний легких. Consilium Medicum 2003; 5 (4): 176–181.
57. Kunitake R., Kuwano K., Yoshida K. et al. KL-6, surfactant protein A and D in bronchoalveolar lavage fluid from patients with pulmonary sarcoidosis. Respiration 2001; 68: 488–495.
58. Kucejko W., Chyczewska E., Naumnik W., Ossolinska M. Concentration of surfactant protein D, Clara cell protein CC-16 and IL-10 in bronchoalveolar lavage (BAL) in patients with sarcoidosis, hypersensivity pneumonitis and idiopathic pulmonary fibrosis. Folia Histochem. Cytobiol. 2009; 47 (2): 225–230.
59. Zissel G., Prasse A., Muller5Quernheim J. Sarcoidosisimmunopathogenetic concepts. J. Semin. Respir. Crit. Care Med. 2007; 28 (1): 3–14.
60. Prasse A., Georges C.G., Biller H. et al. Тh1 cytokine pattern in sarcoidosis is expressed by bronchoalveolar CD4+ and CD8+ T cells. Clin. Exp. Immunol. 2000; 122 (2): 241–248.
Рецензия
Для цитирования:
Малышев И.Ю., Лямина С.В., Шимшелашвили Ш.Л., Вассерман Е.Н. Функциональные ответы альвеолярных макрофагов, сурфактантный белок D и заболевания легких. Пульмонология. 2011;(3):101-107. https://doi.org/10.18093/0869-0189-2011-0-3-101-107
For citation:
Malyshev I.Yu., Lyamina S.V., Shimshelashvili Sh.L., Vasserman E.N. Functions of alveolar macrophages and surfactant protein D in lung disease. PULMONOLOGIYA. 2011;(3):101-107. (In Russ.) https://doi.org/10.18093/0869-0189-2011-0-3-101-107